TY - JOUR
T1 - Observing the cell in its native state
T2 - Imaging subcellular dynamics in multicellular organisms
AU - Liu, Tsung Li
AU - Upadhyayula, Srigokul
AU - Milkie, Daniel E.
AU - Singh, Ved
AU - Wang, Kai
AU - Swinburne, Ian A.
AU - Mosaliganti, Kishore R.
AU - Collins, Zach M.
AU - Hiscock, Tom W.
AU - Shea, Jamien
AU - Kohrman, Abraham Q.
AU - Medwig, Taylor N.
AU - Dambournet, Daphne
AU - Forster, Ryan
AU - Cunniff, Brian
AU - Ruan, Yuan
AU - Yashiro, Hanako
AU - Scholpp, Steffen
AU - Meyerowitz, Elliot M.
AU - Hockemeyer, Dirk
AU - Drubin, David G.
AU - Martin, Benjamin L.
AU - Matus, David Q.
AU - Koyama, Minoru
AU - Megason, Sean G.
AU - Kirchhausen, Tom
AU - Betzig, Eric
N1 - Publisher Copyright:
© 2017 The Authors.
PY - 2018/4/20
Y1 - 2018/4/20
N2 - True physiological imaging of subcellular dynamics requires studying cells within their parent organisms, where all the environmental cues that drive gene expression, and hence the phenotypes that we actually observe, are present. A complete understanding also requires volumetric imaging of the cell and its surroundings at high spatiotemporal resolution, without inducing undue stress on either. We combined lattice light-sheet microscopy with adaptive optics to achieve, across large multicellular volumes, noninvasive aberration-free imaging of subcellular processes, including endocytosis, organelle remodeling during mitosis, and the migration of axons, immune cells, and metastatic cancer cells in vivo. The technology reveals the phenotypic diversity within cells across different organisms and developmental stages and may offer insights into how cells harness their intrinsic variability to adapt to different physiological environments.
AB - True physiological imaging of subcellular dynamics requires studying cells within their parent organisms, where all the environmental cues that drive gene expression, and hence the phenotypes that we actually observe, are present. A complete understanding also requires volumetric imaging of the cell and its surroundings at high spatiotemporal resolution, without inducing undue stress on either. We combined lattice light-sheet microscopy with adaptive optics to achieve, across large multicellular volumes, noninvasive aberration-free imaging of subcellular processes, including endocytosis, organelle remodeling during mitosis, and the migration of axons, immune cells, and metastatic cancer cells in vivo. The technology reveals the phenotypic diversity within cells across different organisms and developmental stages and may offer insights into how cells harness their intrinsic variability to adapt to different physiological environments.
UR - https://www.scopus.com/pages/publications/85045622293
U2 - 10.1126/science.aaq1392
DO - 10.1126/science.aaq1392
M3 - Article
C2 - 29674564
AN - SCOPUS:85045622293
SN - 0036-8075
VL - 360
JO - Science
JF - Science
IS - 6386
M1 - eaaq1392
ER -